Elvitegravir
This antiviral medication blocks an enzyme that the HIV virus needs to insert its genetic material into human cells. It is always used as part of a combination antiretroviral therapy regimen.
Peso Molecular
447,9000 g/mol
LogP
5,30
TPSA
87,10 Ų
Regra dos 5 de Lipinski
Aprovado
Áreas Terapêuticas
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Estrutura 2D
Cite this structure
Embed this structure
SMILES
COc1cc2c(cc1Cc1cccc(Cl)c1F)c(=O)c(C(=O)O)cn2[C@H](CO)C(C)C
InChI
InChI=1S/C23H23ClFNO5/c1-12(2)19(11-27)26-10-16(23(29)30)22(28)15-8-14(20(31-3)9-18(15)26)7-13-5-4-6-17(24)21(13)25/h4-6,8-10,12,19,27H,7,11H2,1-3H3,(H,29,30)/t19-/m1/s1
Molecular Formula
C23H23ClFNO5
HBD / HBA
2 / 7
Ligações Rotacionáveis
7
Átomos Pesados
31
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
Perguntas frequentes
This antiviral medication blocks an enzyme that the HIV virus needs to insert its genetic material into human cells. It is always used as part of a combination antiretroviral therapy regimen.
Yes, Elvitegravir is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL204656. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 5277135. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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